Canonical Allele Identifier: CA452987661
Gene: ESR1 HGNC NCBI

Linked Data

dbSNP Id: rs2128527767
MyVariant Identifiers: chr6:g.152265453G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151944318G>A , CM000668.2:g.151944318G>A GRCh38
NC_000006.11:g.152265453G>A , CM000668.1:g.152265453G>A GRCh37
NC_000006.10:g.152307146G>A NCBI36
NG_008493.1:g.258823G>A
NG_008493.2:g.292628G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000206249.8:c.906G>A MANE Select ENSP00000206249.3:p.Lys302=
ENST00000638569.1:c.42+69G>A ENSP00000491412.1:n.42+69G>A
ENST00000641399.1:n.234G>A
ENST00000206249.7:c.906G>A ENSP00000206249.3:p.Lys302=
ENST00000338799.9:c.906G>A ENSP00000342630.5:p.Lys302=
ENST00000406599.5:c.453-116673G>A ENSP00000384064.1:n.453-116673G>A
ENST00000415488.1:c.115+63547G>A ENSP00000401995.1:n.115+63547G>A
ENST00000427531.6:c.387G>A ENSP00000394721.2:p.Lys129=
ENST00000440973.5:c.906G>A ENSP00000405330.1:p.Lys302=
ENST00000443427.5:c.906G>A ENSP00000387500.1:p.Lys302=
ENST00000456483.3:c.*110+63547G>A ENSP00000415934.3:n.*110+63547G>A
ENST00000482101.1:n.147G>A
NM_000125.3:c.906G>A NP_000116.2:p.Lys302=
NM_001122740.1:c.906G>A NP_001116212.1:p.Lys302=
NM_001122741.1:c.906G>A NP_001116213.1:p.Lys302=
NM_001122742.1:c.906G>A NP_001116214.1:p.Lys302=
NM_001291230.1:c.912G>A NP_001278159.1:p.Lys304=
NM_001291241.1:c.903G>A NP_001278170.1:p.Lys301=
XM_006715374.2:c.906G>A XP_006715437.1:p.Lys302=
XM_006715375.2:c.387G>A XP_006715438.1:p.Lys129=
XM_011535543.1:c.906G>A XP_011533845.1:p.Lys302=
XM_011535544.1:c.906G>A XP_011533846.1:p.Lys302=
XM_011535545.1:c.906G>A XP_011533847.1:p.Lys302=
XM_011535546.1:c.906G>A XP_011533848.1:p.Lys302=
XM_011535547.1:c.906G>A XP_011533849.1:p.Lys302=
XM_011535548.1:c.387G>A XP_011533850.1:p.Lys129=
XM_011535549.1:c.177G>A XP_011533851.1:p.Lys59=
NM_001328100.1:c.387G>A NP_001315029.1:p.Lys129=
XM_006715374.3:c.906G>A XP_006715437.1:p.Lys302=
XM_006715375.3:c.387G>A XP_006715438.1:p.Lys129=
XM_011535543.2:c.906G>A XP_011533845.1:p.Lys302=
XM_011535544.2:c.906G>A XP_011533846.1:p.Lys302=
XM_011535545.2:c.906G>A XP_011533847.1:p.Lys302=
XM_011535547.2:c.906G>A XP_011533849.1:p.Lys302=
XM_011535549.2:c.177G>A XP_011533851.1:p.Lys59=
XM_017010376.1:c.906G>A XP_016865865.1:p.Lys302=
XM_017010377.1:c.906G>A XP_016865866.1:p.Lys302=
XM_017010378.1:c.906G>A XP_016865867.1:p.Lys302=
XM_017010379.1:c.906G>A XP_016865868.1:p.Lys302=
XM_017010380.1:c.906G>A XP_016865869.1:p.Lys302=
XM_017010381.1:c.906G>A XP_016865870.1:p.Lys302=
XM_017010382.2:c.249G>A XP_016865871.1:p.Lys83=
XM_017010383.1:c.117G>A XP_016865872.1:p.Lys39=
XR_001743223.2:n.1276G>A
XR_002956266.1:n.1276G>A
NM_000125.4:c.906G>A MANE Select NP_000116.2:p.Lys302=
NM_001328100.2:c.387G>A NP_001315029.1:p.Lys129=
NM_001122740.2:c.906G>A NP_001116212.1:p.Lys302=
NM_001122741.2:c.906G>A NP_001116213.1:p.Lys302=
NM_001122742.2:c.906G>A NP_001116214.1:p.Lys302=
NM_001291230.2:c.912G>A NP_001278159.1:p.Lys304=
NM_001291241.2:c.903G>A NP_001278170.1:p.Lys301=
NM_001385568.1:c.906G>A NP_001372497.1:p.Lys302=
NM_001385569.1:c.906G>A NP_001372498.1:p.Lys302=
NM_001385570.1:c.906G>A NP_001372499.1:p.Lys302=
NM_001385571.1:c.906G>A NP_001372500.1:p.Lys302=
NM_001385572.1:c.906G>A NP_001372501.1:p.Lys302=